Halovir D
AlkaPlorer ID: AK046068
Synonym: None
IUPAC Name: 2-[[(2S)-2-[[2-[[(2S,4S)-1-[2-(dodecanoylamino)-2-methylpropanoyl]-4-hydroxypyrrolidine-2-carbonyl]amino]-4-methylpentanoyl]amino]-3-methylbutanoyl]amino]-N-[(2S)-1-hydroxy-4-methylpentan-2-yl]pentanediamide
Structure
SMILES: CCCCCCCCCCCC(O)=NC(C)(C)C(=O)N1C[C@@H](O)C[C@H]1C(O)=NC(CC(C)C)C(O)=N[C@H](C(O)=NC(CCC(=N)O)C(O)=N[C@H](CO)CC(C)C)C(C)C
InChI: InChI=1S/C43H79N7O9/c1-10-11-12-13-14-15-16-17-18-19-36(54)49-43(8,9)42(59)50-25-31(52)24-34(50)40(57)47-33(23-28(4)5)39(56)48-37(29(6)7)41(58)46-32(20-21-35(44)53)38(55)45-30(26-51)22-27(2)3/h27-34,37,51-52H,10-26H2,1-9H3,(H2,44,53)(H,45,55)(H,46,58)(H,47,57)(H,48,56)(H,49,54)/t30-,31-,32?,33?,34-,37-/m0/s1
InChIKey: XLHSKXDZYNSELH-NUNUOSAZSA-N
Reference
Halovirs A–E, new antiviral agents from a marine-Derived fungus of the genus Scytalidium
PubChem CID: 21777387
LOTUS: LTS0218455
{NPAtlas: NPA002673
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Scytalidium sp. | Scytalidium | None | None | Leotiomycetes | Ascomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 838.145
TPSA？: 267.79999999999995
MolLogP？: 7.960570000000008
Number of H-Donors: 9
Number of H-Acceptors: 9
RingCount: 1
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|